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1.
World Neurosurg ; 90: 704.e11-704.e18, 2016 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-26960276

RESUMO

BACKGROUND: Intraventricular ependymal cysts (ECs) are rare, histologically benign neuroepithelial cysts. Most of these cysts are clinically silent and discovered incidentally. Rarely, they become symptomatic, leading to obstruction of the cerebrospinal fluid circulation. ECs located inside the ventricles may manifest with signs of increased intracranial pressure. CASE DESCRIPTION: A 32-year-old woman presented with a 6-year history of tremor affecting her left hand. In the last month, she had been experiencing headache as well, and the tremor of the left hand was affecting her quality of life. The patient demonstrated a fine resting and intention tremor of the left hand and a voice tremor. Magnetic resonance imaging revealed a large cystic, nonenhancing lesion within the right lateral ventricle. The fluid within the cyst was isointense to cerebrospinal fluid on all sequences. Because of the rapid progression of her symptoms and no response to medication, surgical decompression of the cyst was considered. The cyst was removed by an endoscope-assisted microsurgical technique. Her postoperative course was uneventful. A marked reduction in her tremor was noted in the immediate postoperative period. Histopathologic diagnosis was of an EC. During the follow-up period, the patient's tremor, although still present, had improved dramatically. At 6 months postoperatively, she could hold a drinking glass without spilling. CONCLUSIONS: This is a unique case of an intraventricular EC that manifested with tremor, which improved by endoscope-assisted microsurgical removal of the cyst. This case also supports the important role of endoscopic surgery in the treatment of intraventricular cystic lesions.


Assuntos
Cistos do Sistema Nervoso Central/cirurgia , Neoplasias do Ventrículo Cerebral/cirurgia , Microcirurgia/métodos , Neuroendoscopia/métodos , Tremor/prevenção & controle , Adulto , Cistos do Sistema Nervoso Central/complicações , Neoplasias do Ventrículo Cerebral/complicações , Neoplasias do Ventrículo Cerebral/patologia , Ventrículos Cerebrais/patologia , Ventrículos Cerebrais/cirurgia , Epêndima/patologia , Epêndima/cirurgia , Feminino , Humanos , Resultado do Tratamento , Tremor/diagnóstico , Tremor/etiologia
2.
Eurasian J Med ; 47(3): 174-8, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26644765

RESUMO

OBJECTIVE: Myelomeningoceles are the common form of open neural tube defects that are usually associated with neurological deficits. Many techniques of repair and methods of prevention have been proposed with respect to the size of defect and the neurological condition of patient. The aim of this study was to report our experience on the management of lumbosacral myelomeningoceles in children. MATERIALS AND METHODS: We retrospectively analysed the data of 36 paediatric cases of surgically lumbosacral myelomeningocele treated in our department between 1998 and 2013. Twenty (56%) patients were female and sixteen were male, with a mean age of 4 months (ranged between 0 and 24 months). All patients had neurological deficits in the preoperative period. Computed tomography was performed in 33 (92%) patients and magnetic resonance imaging in 15 (42%) patients in the preoperative period. Repair of the myelomeningocele and closure of the skin defect were performed in all patients. The mean follow-up period was 36 months. RESULTS: Thirty (83%) patients were operated for hydrocephalus and 10 (28%) patients were re-operated for tethered cord syndrome during the follow-up period. Neurological worsening was not observed in any patient while cerebrospinal fluid fistula was detected in 2 patients. CONCLUSION: Surgical treatment using appropriate microsurgical techniques is crucial for lumbosacral myelomeningoceles in children. Early surgical intervention with close follow-up will improve the neurological condition of the patients.

3.
Neurosurgery ; 11 Suppl 2: 213-9, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25950887

RESUMO

BACKGROUND: The procedure of reconstruction after the removal of cranial fibrous dysplasia (FD) must be precise to achieve good functional and aesthetic results. Intraoperative modeling of implants is difficult and may cause cosmetic disturbances. OBJECTIVE: To present our experience with the treatment of cranial FD using preoperative computer-based surgical planning of tumor removal with reconstruction of the cranium with custom-made titanium implants. METHODS: Four patients underwent surgical treatment for cranial FD over a 2-year period. All patients were male with a mean age of 25.25 years and had monostotic-type FD. Computed tomography (CT) with 0.5-mm slices was obtained preoperatively. Computer-based planning of the tumor removal was performed, and a template was created by the computer to determine the margins of tumor removal. After this procedure, the preoperative computer-based construction of the titanium implant was performed. The patients underwent surgical treatment, and the tumor was removed with the use of this template. Then, the titanium implant was inserted onto the bone defect and fixed with mini-screws. Patients were followed up by periodic CT scans. RESULTS: The histological diagnosis of all patients was FD. No intraoperative or postoperative complications have occurred. Postoperative CT scans showed complete tumor removal and confirmed appropriate cosmetic reconstruction. The mean follow-up period was 15.25 months. CONCLUSION: Computer-based surgical planning associated with the production of custom-made titanium implants is a highly promising method for the treatment of cranial FD. Better radiological and cosmetic outcomes could be obtained by this technique with interdisciplinary work with medical designers.


Assuntos
Displasia Fibrosa Óssea/cirurgia , Procedimentos de Cirurgia Plástica/instrumentação , Próteses e Implantes , Cirurgia Assistida por Computador/métodos , Titânio , Adulto , Humanos , Masculino , Procedimentos de Cirurgia Plástica/métodos , Crânio/cirurgia , Tomografia Computadorizada por Raios X , Adulto Jovem
4.
Turk Neurosurg ; 24(6): 859-66, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25448201

RESUMO

AIM: Surgical removal of sphenoorbital meningiomas is challenging for neurosurgeons. The aim of study is to share our experience on sphenoorbital meningiomas and to provide a picture of the current state of the art in surgical treatment of these tumors. MATERIAL AND METHODS: The data of 13 cases of sphenoorbital meningioma who were operated between 2006 and 2013 was reviewed retrospectively. Intraorbital extension was present in 10 cases while sphenoid bone invasion was detected in 9 cases. All patients underwent surgical treatment after the radiological evaluation with magnetic resonance imaging and computed tomography. The degree of resection and the clinical outcome of all patients were analyzed. RESULTS: Extended pterional approach with a large frontotemporal craniotomy was performed in all cases. Simpson's grade I and II excision was achieved in 4 (31%) cases while subtotal excision (Simpson's grade III or higher) was performed in 9 cases. The main reason for subtotal excision was the cavernous sinus invasion. Optic canal decompression was performed in patients with intraorbital invasion. CONCLUSION: Although total removal is the main objective of surgery, the sphenoorbital meningiomas are difficult to resect especially with cavernous sinus invasion. But in the meantime, it is not recommended to take any excessive risks to achieve a greater degree of resection for a benign tumor. Endoscopic approach is an option for inferomedial orbital parts of these tumors.


Assuntos
Neoplasias Meníngeas/cirurgia , Meningioma/cirurgia , Procedimentos Neurocirúrgicos/métodos , Neoplasias Orbitárias/cirurgia , Adulto , Seio Cavernoso/patologia , Seio Cavernoso/cirurgia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Osso Esfenoide/patologia , Osso Esfenoide/cirurgia , Resultado do Tratamento
5.
Turk Neurosurg ; 24(4): 549-57, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25050681

RESUMO

AIM: We aimed to show the effects of neuronavigation and intraoperative imaging systems on the surgical outcomes of orbital tumors. MATERIAL AND METHODS: Seventeen patients who underwent surgical treatment for orbital tumors by transcranial and transnasal approaches between 2008 and 2013 were analyzed retrospectively. Twelve of them were male and 5 were female. The mean age was 41.6 years. Neuronavigation systems were used in all cases. Four patients were operated using intraoperative imaging systems. RESULTS: The transcranial approach was used in 9 (53%) patients, endoscopic medial orbital approach in 4 (23.5%), endoscopic inferolateral approach in 1 (6%), cranioorbitozygomatic approach in 1, lateral approach in 1, and the combined (medial endoscopic and lateral) approach in 1 patients. Total resection was achieved in 5 patients, gross total excision in 2, subtotal in 9 and partial in 1 patients. CONCLUSION: Modern technology has made a significant contribution to the treatment of orbital tumors. Although technological equipments facilitate the excision of tumors, the level of resection is mainly determined by the nature of tumor and adhesion to the adjacent neurovascular structures. It should not be forgotten that advanced technology never replaces a good anatomical knowledge and surgical experience, but has a complementary role.


Assuntos
Neuroimagem/métodos , Neuronavegação/métodos , Procedimentos Neurocirúrgicos/métodos , Neoplasias Orbitárias/cirurgia , Adulto , Idoso , Pré-Escolar , Feminino , Humanos , Período Intraoperatório , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Exame Neurológico , Estudos Retrospectivos , Tomografia Computadorizada por Raios X , Resultado do Tratamento , Adulto Jovem
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